Literature DB >> 33583360

Inflammation-related adverse reactions following vaccination potentially indicate a stronger immune response.

Chun-Lan Zhuang1, Zhi-Jie Lin2, Zhao-Feng Bi1, Ling-Xian Qiu1, Fang-Fang Hu1, Xiao-Hui Liu1, Bi-Zhen Lin2, Ying-Ying Su1, Hui-Rong Pan2, Tian-Ying Zhang1, Shou-Jie Huang1, Yue-Mei Hu3, You-Lin Qiao4, Feng-Cai Zhu3, Ting Wu1, Jun Zhang1, Ning-Shao Xia1.   

Abstract

Concerns about vaccine safety are an important reason for vaccine hesitancy, however, limited information is available on whether common adverse reactions following vaccination affect the immune response. Data from three clinical trials of recombinant vaccines were used in this post hoc analysis to assess the correlation between inflammation-related solicited adverse reactions (ISARs, including local pain, redness, swelling or induration and systematic fever) and immune responses after vaccination. In the phase III trial of the bivalent HPV-16/18 vaccine (Cecolin®), the geometric mean concentrations (GMCs) for IgG anti-HPV-16 and -18 (P<0.001) were significantly higher in participants with any ISAR following vaccination than in those without an ISAR. Local pain, induration, swelling and systemic fever were significantly correlated with higher GMCs for IgG anti-HPV-16 and/or anti-HPV-18, respectively. Furthermore, the analyses of the immunogenicity bridging study of Cecolin® and the phase III trial of a hepatitis E vaccine yielded similar results. Based on these results, we built a scoring model to quantify the inflammation reactions and found that the high score of ISAR indicates the strong vaccine-induced antibody level. In conclusion, this study suggests inflammation-related adverse reactions following vaccination potentially indicate a stronger immune response.

Entities:  

Keywords:  Inflammation; adverse reaction; antibody; immune response; recombinant vaccine; vaccine hesitancy

Mesh:

Substances:

Year:  2021        PMID: 33583360      PMCID: PMC7928063          DOI: 10.1080/22221751.2021.1891002

Source DB:  PubMed          Journal:  Emerg Microbes Infect        ISSN: 2222-1751            Impact factor:   7.163


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